A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies
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author: Sarah K. Westbury, Myrto Kostadima, Sylvia Richardson, Willem H. Ouwehand, Sol Schulman, Augusto Rendon, Ernest Turro, John R Bradley, Kathleen Freson, Wendy Erber, Marc De Maeyer, Johan W.M. Heemskerk
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